Disease #03845

Official abbreviation MC3DN-5
Name mitochondrial complex III deficiency, nuclear type 5 (MC3DN-5)
OMIM ID 615160
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene UQCRC2
Associated tissues -
Disease features -
Remarks -